scholarly journals Long-term implicit memory for sequential auditory patterns in humans

eLife ◽  
2020 ◽  
Vol 9 ◽  
Author(s):  
Roberta Bianco ◽  
Peter MC Harrison ◽  
Mingyue Hu ◽  
Cora Bolger ◽  
Samantha Picken ◽  
...  
Keyword(s):  
Implicit Memory ◽  
Auditory System ◽  
Memory Formation ◽  
Detection Time ◽  
Multiple Timescales ◽  
Acoustic Environment ◽  
Series Of Experiments ◽  
Behavioural Manipulation ◽  
Repeating Patterns

Memory, on multiple timescales, is critical to our ability to discover the structure of our surroundings, and efficiently interact with the environment. We combined behavioural manipulation and modelling to investigate the dynamics of memory formation for rarely reoccurring acoustic patterns. In a series of experiments, participants detected the emergence of regularly repeating patterns within rapid tone-pip sequences. Unbeknownst to them, a few patterns reoccurred every ~3 min. All sequences consisted of the same 20 frequencies and were distinguishable only by the order of tone-pips. Despite this, reoccurring patterns were associated with a rapidly growing detection-time advantage over novel patterns. This effect was implicit, robust to interference, and persisted for 7 weeks. The results implicate an interplay between short (a few seconds) and long-term (over many minutes) integration in memory formation and demonstrate the remarkable sensitivity of the human auditory system to sporadically reoccurring structure within the acoustic environment.

scholarly journals Long-term implicit memory for sequential auditory patterns in humans

2020 ◽  
Author(s):  
Roberta Bianco ◽  
Peter M. C. Harrison ◽  
Mingyue Hu ◽  
Cora Bolger ◽  
Samantha Picken ◽  
...  
Keyword(s):  
Human Performance ◽  
Long Term Memory ◽  
Sensory Inputs ◽  
Psychological Mechanisms ◽  
Memory Decay ◽  
Series Of Experiments ◽  
Auditory Scenes ◽  
Behavioural Manipulation ◽  
Repeating Patterns

AbstractTo understand auditory scenes, listeners track and retain the statistics of sensory inputs as they unfold over time. We combined behavioural manipulation and modelling to investigate how sequence statistics are encoded into long-term memory and used to interpret incoming sensory signals. In a series of experiments, participants detected the emergence of regularly repeating patterns in novel rapid sound sequences. Unbeknownst to them, a few regular patterns reoccurred sparsely (every ∼3 minutes). Reoccurring sequences showed a rapidly growing detection time advantage over novel sequences. This effect was implicit, robust to interference, and persisted up to 7 weeks. Human performance was reproduced by a memory-constrained probabilistic model, where sequences are stored as n-grams and are subject to memory decay. Results suggest that similar psychological mechanisms may underlie integration processes over different-time scales in memory formation and flexible retrieval.

scholarly journals Disruption of the astrocyte–neuron interaction is responsible for the impairments in learning and memory in 5XFAD mice: an Alzheimer’s disease animal model

2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Moonseok Choi ◽  
Sang-Min Lee ◽  
Dongsoo Kim ◽  
Heh-In Im ◽  
Hye-Sun Kim ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Animal Model ◽  
Memory Formation ◽  
Long Term Memory ◽  
Term Memory ◽  
Stat3 Phosphorylation ◽  
Neuron Interactions ◽  
5Xfad Mice

AbstractThe morphological dynamics of astrocytes are altered in the hippocampus during memory induction. Astrocyte–neuron interactions on synapses are called tripartite synapses. These control the synaptic function in the central nervous system. Astrocytes are activated in a reactive state by STAT3 phosphorylation in 5XFAD mice, an Alzheimer’s disease (AD) animal model. However, changes in astrocyte–neuron interactions in reactive or resting-state astrocytes during memory induction remain to be defined. Here, we investigated the time-dependent changes in astrocyte morphology and the number of astrocyte–neuron interactions in the hippocampus over the course of long-term memory formation in 5XFAD mice. Hippocampal-dependent long-term memory was induced using a contextual fear conditioning test in 5XFAD mice. The number of astrocytic processes increased in both wild-type and 5XFAD mice during memory formation. To assess astrocyte–neuron interactions in the hippocampal dentate gyrus, we counted the colocalization of glial fibrillary acidic protein and postsynaptic density protein 95 via immunofluorescence. Both groups revealed an increase in astrocyte–neuron interactions after memory induction. At 24 h after memory formation, the number of tripartite synapses returned to baseline levels in both groups. However, the total number of astrocyte–neuron interactions was significantly decreased in 5XFAD mice. Administration of Stattic, a STAT3 phosphorylation inhibitor, rescued the number of astrocyte–neuron interactions in 5XFAD mice. In conclusion, we suggest that a decreased number of astrocyte–neuron interactions may underlie memory impairment in the early stages of AD.

scholarly journals Protein kinase D promotes plasticity-induced F-actin stabilization in dendritic spines and regulates memory formation

2015 ◽  
Vol 210 (5) ◽  
pp. 771-783 ◽  
Author(s):  
Norbert Bencsik ◽  
Zsófia Szíber ◽  
Hanna Liliom ◽  
Krisztián Tárnok ◽  
Sándor Borbély ◽  
...  
Keyword(s):  
Synaptic Plasticity ◽  
Protein Kinase ◽  
Dendritic Spines ◽  
Morphological Changes ◽  
Long Term Potentiation ◽  
Memory Formation ◽  
Protein Kinase D

Actin turnover in dendritic spines influences spine development, morphology, and plasticity, with functional consequences on learning and memory formation. In nonneuronal cells, protein kinase D (PKD) has an important role in stabilizing F-actin via multiple molecular pathways. Using in vitro models of neuronal plasticity, such as glycine-induced chemical long-term potentiation (LTP), known to evoke synaptic plasticity, or long-term depolarization block by KCl, leading to homeostatic morphological changes, we show that actin stabilization needed for the enlargement of dendritic spines is dependent on PKD activity. Consequently, impaired PKD functions attenuate activity-dependent changes in hippocampal dendritic spines, including LTP formation, cause morphological alterations in vivo, and have deleterious consequences on spatial memory formation. We thus provide compelling evidence that PKD controls synaptic plasticity and learning by regulating actin stability in dendritic spines.

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